Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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Philips has determined that there is a need to make all owners aware that it is important to call their local philips representative for technical support if any of their aeds have ever emitted or begin toemit a pattern of triple chirps. even if the user is able to clear the triple-chirp condition the device may require additional investigation.